Relevant bibliographies by topics / PROTEIN N

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'PROTEIN N'

Author: Grafiati
Published: 11 September 2023
Last updated: 31 July 2025

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Journal articles on the topic "PROTEIN N"

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Duclos, S., P. Da Silva, F. Vovelle, F. Piller, and V. Piller. "Characterization of the UDP-N-acetylgalactosamine binding domain of bovine polypeptide N-acetylgalactosaminyltransferase T1." Protein Engineering Design and Selection 17, no. 8 (2004): 635–46. http://dx.doi.org/10.1093/protein/gzh075.

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Koyama, Y., M. Hidaka, M. Nishimoto, and M. Kitaoka. "Directed evolution to enhance thermostability of galacto-N-biose/lacto-N-biose I phosphorylase." Protein Engineering Design and Selection 26, no. 11 (2013): 755–61. http://dx.doi.org/10.1093/protein/gzt049.

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Gordon, J. I., R. J. Duronio, D. A. Rudnick, S. P. Adams, and G. W. Gokel. "Protein N-myristoylation." Journal of Biological Chemistry 266, no. 14 (1991): 8647–50. http://dx.doi.org/10.1016/s0021-9258(18)31490-x.

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Flanagan, Karen, John Walshaw, Sarah L. Price, and Julia M. Goodfellow. "Solvent interactions with n ring systems in proteins." "Protein Engineering, Design and Selection" 8, no. 2 (1995): 109–16. http://dx.doi.org/10.1093/protein/8.2.109.

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Imberty, A., and S. Perez. "Stereochemistry of the N-glycosylation sites in glycoproteins." Protein Engineering Design and Selection 8, no. 7 (1995): 699–709. http://dx.doi.org/10.1093/protein/8.7.699.

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Roth, Jürgen, Christian Zuber, Sujin Park, et al. "Protein N-glycosylation, protein folding, and protein quality control." Molecules and Cells 30, no. 6 (2010): 497–506. http://dx.doi.org/10.1007/s10059-010-0159-z.

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Hollebeke, Jolien, Petra Van Damme та Kris Gevaert. "N-terminal acetylation and other functions of Nα-acetyltransferases". Biological Chemistry 393, № 4 (2012): 291–98. http://dx.doi.org/10.1515/hsz-2011-0228.

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Abstract Protein N-terminal acetylation by Nα-acetyltransferases (NATs) is an omnipresent protein modification that affects a large number of proteins. The exact biological role of N-terminal acetylation has, however, remained enigmatic for the overall majority of affected proteins, and only for a rather small number of proteins, N-terminal acetylation was linked to various protein features including stability, localization, and interactions. This minireview tries to summarize the recent progress made in understanding the functionality of N-terminal protein acetylation and also focuses on nonc
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Hope, John N., Hao-Chia Chen та J. Fidding Hejtmancik. "βA3/Al-crystallin association: role of the N-terminal arm". "Protein Engineering, Design and Selection" 7, № 3 (1994): 445–51. http://dx.doi.org/10.1093/protein/7.3.445.

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Wu, Di, Weston B. Struwe, David J. Harvey, Michael A. J. Ferguson, and Carol V. Robinson. "N-glycan microheterogeneity regulates interactions of plasma proteins." Proceedings of the National Academy of Sciences 115, no. 35 (2018): 8763–68. http://dx.doi.org/10.1073/pnas.1807439115.

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Altered glycosylation patterns of plasma proteins are associated with autoimmune disorders and pathogenesis of various cancers. Elucidating glycoprotein microheterogeneity and relating subtle changes in the glycan structural repertoire to changes in protein–protein, or protein–small molecule interactions, remains a significant challenge in glycobiology. Here, we apply mass spectrometry-based approaches to elucidate the global and site-specific microheterogeneity of two plasma proteins: α1-acid glycoprotein (AGP) and haptoglobin (Hp). We then determine the dissociation constants of the anticoag
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Doughty, S. W., F. E. Blaney, B. S. Orlek, and W. G. Richards. "A molecular mechanism for toxin block in N-type calcium channels." Protein Engineering Design and Selection 11, no. 2 (1998): 95–99. http://dx.doi.org/10.1093/protein/11.2.95.

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Dissertations / Theses on the topic "PROTEIN N"

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Lundell, Sandra J. "Quantum Mechanical Studies of N-H···N Hydrogen Bonding in Acetamide Derivatives and Amino Acids." DigitalCommons@USU, 2018. https://digitalcommons.usu.edu/etd/7309.

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Proteins are made of vast chains of amino acids that twist and fold into intricate designs. These structures are held in place by networks of noncovalent interactions. One of these, the hydrogen bond, forms bridges between adjacent pieces of the protein chain and is one of the most important contributors to the shape and stability of proteins. Hydrogen bonds come in all shapes and sizes and a full understanding of these not only aids in our understanding of proteins in general but can bridge the gap to finding cures to many protein-related diseases, such as sickle-cell anemia. The primary aim
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Agah, Sayeh. "Parvalbumin stability and calcium affinity : the impact of the n-terminal domain /." Free to MU Campus, others may purchase, 2004. http://wwwlib.umi.com/cr/mo/fullcit?3164486.

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Huffman, Jennifer Elizabeth. "Genetic analysis of protein N-glycosylation." Thesis, University of Edinburgh, 2014. http://hdl.handle.net/1842/10038.

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The majority of human proteins are post-translationally modified by covalent addition of one or more complex oligosaccharides (glycans). Alterations in glycosylation processing are associated with numerous diseases and glycans are attracting increasing attention both as disease biomarkers and as targets for novel therapeutic approaches. Using a recently developed high performance liquid chromatography (HPLC) method for high-throughput glycan analysis, genome-wide association studies (GWAS) of 33 directly measured and 13 derived N-glycan features were performed in 3533 individuals from four Eur
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Lucas, Olivier. "Molecular and systemic functions of the vertebrate-specific TATA-binding protein N terminus." Diss., Montana State University, 2009. http://etd.lib.montana.edu/etd/2009/lucas/LucasO0509.pdf.

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Woollard, Geoffrey Robert Paget. "Redesign of the N-end rule protein ClpS for use in high-throughput N-end protein sequencing." Thesis, University of British Columbia, 2014. http://hdl.handle.net/2429/46377.

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Current protein sequencing methods include mass spectrometry and Edman degradation. We envision a novel high-throughput protein sequencing method using affinity adapters to recognize the N-terminal residue of a denatured peptide in an iterative process. This thesis takes a first step toward designing robust and selective affinity reagents. We outline our pipeline for designing selective protein adapters that recognize the N-terminal amino acid of a peptide independent of the following sequence. We based our design on a substrate recognition protein in the N-end rule pathway, ClpS. The bacteria
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Wood, Alison. "N-linked protein glycosylation in Helicobacter species." Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/nlinked-protein-glycosylation-in-helicobacter-species(ef97ffdd-aca4-40ff-b52b-7b8ca030bc82).html.

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N-linked protein glycosylation involves the transfer of a glycan onto an Asparagine residue (N) of a polypeptide chain. It is common in Eukaryotes and has recently been observed in Prokaryotes, most notably in Campylobacter jejuni. The C. jejuni N-linked glycosylation system is encoded on a single pgl gene locus that also functions when expressed in Escherichia coli. The key enzyme involved in N-linked protein glycosylation is encoded by the pglB gene and transfers lipid-linked glycan onto N residues of glycoproteins in the periplasm. It is clear from accumulating genome sequence data that pgl
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Karlsson, Gunilla Birgitta. "Effects of the imino sugar N-butyldeoxynojirimycin on protein N-linked glycosylation." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333246.

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Raggett, Elaine. "The structure and function of translocation domain of Colicin N." Thesis, University of Newcastle Upon Tyne, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.285400.

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Murray, Anne Riché. "The functional significance of rhodopsin's N-linked glycosylation." Oklahoma City : [s.n.], 2009.

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Su, Wei. "Characterization of N-GAIP, a novel RGS protein." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape10/PQDD_0010/MQ40774.pdf.

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Books on the topic "PROTEIN N"

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Su, Wei. Characterization of N-GAIP, a novel RGS protein. National Library of Canada, 1998.

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Ravi, Iyengar, and Birnbaumer Lutz, eds. G proteins. Academic Press, 1990.

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Raouf, Ramin K. Functional regulation of N-methyl-D-aspartate receptors by serine/threonine protein kinases. National Library of Canada = Bibliothèque nationale du Canada, 1999.

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Verfasser, Schließmann Stephan J., Kirschbaum Andreas Verfasser, Plönes Till 1976 Verfasser, et al., eds. Roflumilast-N-oxide induces surfactant protein expression in human alveolar epithelial cells type II. Universität, 2012.

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Bartlett, Mary Claire. Modulation of N-methyl-D-aspartate currents in cultured hippocampal neurones by protein kinase C. National Library of Canada = Bibliothèque nationale du Canada, 1992.

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Mah, Thien-Fah. The interaction between E. coli protein NusA and the N-nut site complex bacteriophage [lambda]. National Library of Canada, 1994.

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Konarski, Jakub Z. Molecular mechanism of protein kinase C enhancement of N-methyl-D-aspartate receptor calcium-dependent inactivation. National Library of Canada, 2002.

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Karlsruhe, Universität, ed. Strategien zur 13C-Myristoylcarbadethiacoenzym A-Synthese: Darstellung neuer potentieller Inhibitoren des Enzyms Myristoylcoenzym A: Protein N-Myristoyltransferase. [s.n.], 1997.

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Pieribone, Vincent. Aglow in the dark: The revolutionary science of biofluorescence. Belknap Press of Harvard University Press, 2005.

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Martin, R. P. Synthesis of a thiosugar analogue of an N - linked oligosaccharide fragment: A tool for the study of carbohydrate -protein interactions. UMIST, 1995.

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Book chapters on the topic "PROTEIN N"

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Schomburg, Dietmar, and Dörte Stephan. "Protein N-acetylglucosaminyltransferase." In Enzyme Handbook 12. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61117-9_97.

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Ciechanover, Aaron. "N-terminal Ubiquitination: No Longer Such a Rare Modification." In Protein Degradation. Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/352760586x.ch2.

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Bill, Roslyn M., Leigh Revers, and Iain B. H. Wilson. "Core Issues: Building The Groundwork for N-Linked Sugars." In Protein Glycosylation. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4939-0_4.

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Bill, Roslyn M., Leigh Revers, and Iain B. H. Wilson. "Branching Out: Constructing The Antennae Of N-Linked Sugars." In Protein Glycosylation. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-4939-0_5.

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Benoiton, N. Leo. "Update on the Synthesis of N-Methyl Amino Acids." In Protein Methylation. CRC Press, 2024. https://doi.org/10.1201/9781003574873-19.

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Hirano, Hisashi, and Roza M. Kamp. "Deblocking of N-Terminally Modified Proteins." In Protein Sequencing Protocols. Humana Press, 2003. http://dx.doi.org/10.1385/1-59259-342-9:355.

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Schomburg, Dietmar, and Dörte Stephan. "Protein-arginine N-methyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_23.

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Schomburg, Dietmar, and Dörte Stephan. "Protein-histidine N-methyltransferase." In Enzyme Handbook 11. Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/978-3-642-61030-1_81.

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Zhang, Jiapu. "Nucleocapsid Phosphoprotein (N-Protein)." In Springer Series in Biophysics. Springer Nature Switzerland, 2023. http://dx.doi.org/10.1007/978-3-031-36773-1_22.

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Jackson, Philip J. "N-Terminal Protein Sequencing for Special Applications." In Protein Sequencing Protocols. Humana Press, 2003. http://dx.doi.org/10.1385/1-59259-342-9:287.

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Conference papers on the topic "PROTEIN N"

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Rizqiana, Annisa, and Afiahayati. "Protein Secondary Structure Prediction using N-Grams and 1-Dimensional Convolutional Neural Network." In 2024 Joint 13th International Conference on Soft Computing and Intelligent Systems and 25th International Symposium on Advanced Intelligent Systems (SCIS&ISIS). IEEE, 2024. https://doi.org/10.1109/scisisis61014.2024.10759947.

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AEBI, MARKUS. "N-LINKED PROTEIN GLYCOSYLATION." In 23rd International Solvay Conference on Chemistry. WORLD SCIENTIFIC, 2014. http://dx.doi.org/10.1142/9789814603836_0023.

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Krul, Elaine. "Nitrogen to Protein Conversion Factors - An update and practical guidance for their use and for determining specific factors for novel protein sources." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/amwx7627.

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Protein content in food is measured indirectly (since the 1880’s) by determining nitrogen (N) and using a nitrogen to protein conversion factor (NPCF). NPCFs were initially based on proteins that were readily available at the time and found to contain about 16% N. Hence, a NPCF of 6.25 (100/16) was applied to all proteins, assuming all N was from amino acids (AAs). Recent technological advances revealed differences in AA composition and content of non-protein N between proteins indicating that an NPCF of 6.25 overestimates the protein content of most foods. However, 6.25 is still widely used.
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Jundt, Emily, Kaustav Majumder, and Bijesh Maharjan. "Does Soil Nutrient Management with Nitrogen Fertilizer Increase Protein Content in Leguminous Plants." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/qgrx4847.

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Dry edible beans (Phaseolus vulgaris) are leguminous plants and are an excellent source of dietary proteins. Great Northern (GN) beans are a market class of dry edible beans and a major agricultural commodity in Nebraska. Soil nutrient management with nitrogen (N) fertilizer can enhance bean production by increasing N uptake, potentially improving protein quantity, and resulting in a potential economic benefit to bean farmers. Thus, this experiment aims to evaluate and optimize the effects of N treatment on yield, total protein, and soluble protein in GN beans. Seven treatments were tested, co
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Marshall, Glenn M., Pei Y. Liu, Samuele Gherardi, et al. "Abstract 3027: SIRT1 promotes N-Myc oncogenesis stabilizing N-Myc protein." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-3027.

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Hopmeier, P., M. Halbmayer, H. P. Schwarz, F. Heuss, and M. Fischer. "PROTEIN C AND PROTEIN S IN MILD AND MODERATE PREECLAMPSIA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644285.

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In normal pregnancy, total protein S antigen and activity have been reported to be markedly reduced, whereas protein C level was found unaltered. In contrast, in severe preeclampsia protein C antigen was found to be considerably reduced. The presentstudy was done to clarify whether similar changes in protein Cwould alsobe observed for the mildand moderatepreeclamptic state andwhether there would be any effects on the level ofprotein S, since nodata on this cofactor in preeclampsia have been reported to date. 4-0 women in the 3rd trimester of pregnancy - 20 with uncomplicated pregnancies and 20
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Santrer, Emanoelle La, Edgar L. Aguiar, Cláudia B. Assunção, Sandro R. Dias, Thiago S. Rodrigues, and Rachel B. Caligiorne. "Computational Assessment of Spike Protein Diversity in SARS-CoV-2 Lineages." In v. 11 n. 1 (2025): CNMAC 2024. SBMAC, 2025. https://doi.org/10.5540/03.2025.011.01.0365.

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Novikova, L. I., S. S. Bochkareva, A. V. Aleshkin, et al. "DYNAMICS OF ANTIBODIES TO VARIOUS ANTIGENS OF THE SARS-COV-2 CORONAVIRUS IN PATIENTS WITH CONFIRMED COVID-19 INFECTION." In Molecular Diagnostics and Biosafety. Federal Budget Institute of Science 'Central Research Institute for Epidemiology', 2020. http://dx.doi.org/10.36233/978-5-9900432-9-9-159.

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Presence of IgG and IgM antibodies in venous blood of 76 patients with confirmed presence of SARS-CoV-2 was determined. The study was carried out by ELISA using Russian test systems. Revealed different levels of IgM antibodies to N-protein and RBD (receptor binding domain of the Spike protein). The level of IgM to RBD did not reach high values, while the level of IgM to N-protein sharply increased in a short period of time to high values by the 3rd week of the disease and decreased only by the 8th week. The dynamics of IgG antibodies to the whole virion antigen and the recombinant spikes was s
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Nasrollahi, S. M., P. Nozière, R. J. Dewhurst, et al. "Natural 15N abundances in plasma and urea-N concentration in milk as biomarkers of urinary N excretion in dairy cows: a meta-analysis." In 6th EAAP International Symposium on Energy and Protein Metabolism and Nutrition. Wageningen Academic Publishers, 2019. http://dx.doi.org/10.3920/978-90-8686-891-9_66.

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Ganapathiraju, M., D. Weisser, R. Rosenfeld, J. Carbonell, R. Reddy, and J. Klein-Seetharaman. "Comparative n-gram analysis of whole-genome protein sequences." In the second international conference. Association for Computational Linguistics, 2002. http://dx.doi.org/10.3115/1289189.1289259.

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Reports on the topic "PROTEIN N"

1

Gumerlock, Paul H. Protein Interaction with the N-Terminus of the Androgen Receptor. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada421196.

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Gumerlock, Paul H. Protein Interaction with the N-Terminus of the Androgen Receptor. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada384350.

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Gafny, Ron, A. L. N. Rao, and Edna Tanne. Etiology of the Rugose Wood Disease of Grapevine and Molecular Study of the Associated Trichoviruses. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7575269.bard.

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Rugose wood is a complex disease of grapevines, characterized by modification of the woody cylinder of affected vines. The control of rugose wood is based on the production of healthy propagation material. Detection of rugose wood in grapevines is difficult and expensive: budwood from tested plants is grafted onto sensitive Vitis indicators and the appearance of symptoms is monitored for 3 years. The etiology of rugose wood is complex and has not yet been elucidated. Several elongated clostero-like viruses are consistently found in affected vines; one of them, grapevine virus A (GVA), is close
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Loebenstein, Gad, William Dawson, and Abed Gera. Association of the IVR Gene with Virus Localization and Resistance. United States Department of Agriculture, 1995. http://dx.doi.org/10.32747/1995.7604922.bard.

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We have reported that localization of TMV in tobacco cultivars with the N gene, is associated with a 23 K protein (IVR) that inhibited replication of several plant viruses. This protein was also found in induced resistant tissue of Nicotiana glutinosa x Nicotiana debneyi. During the present grant we found that TMV production is enhanced in protoplasts and plants of local lesion responding tobacco cultivars exposed to 35oC, parallel to an almost complete suppression of the production of IVR. We also found that IVR is associated with resistance mechanisms in pepper cultivars. We succeeded to clo
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Epel, Bernard L., Roger N. Beachy, A. Katz, et al. Isolation and Characterization of Plasmodesmata Components by Association with Tobacco Mosaic Virus Movement Proteins Fused with the Green Fluorescent Protein from Aequorea victoria. United States Department of Agriculture, 1999. http://dx.doi.org/10.32747/1999.7573996.bard.

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The coordination and regulation of growth and development in multicellular organisms is dependent, in part, on the controlled short and long-distance transport of signaling molecule: In plants, symplastic communication is provided by trans-wall co-axial membranous tunnels termed plasmodesmata (Pd). Plant viruses spread cell-to-cell by altering Pd. This movement scenario necessitates a targeting mechanism that delivers the virus to a Pd and a transport mechanism to move the virion or viral nucleic acid through the Pd channel. The identity of host proteins with which MP interacts, the mechanism
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Varga, Gabriella A., Amichai Arieli, Lawrence D. Muller, Haim Tagari, Israel Bruckental, and Yair Aharoni. Effect of Rumen Available Protein, Amimo Acids and Carbohydrates on Microbial Protein Synthesis, Amino Acid Flow and Performance of High Yielding Cows. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7568103.bard.

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The effect of rumen available protein amino acids and carbohydrates on microbial protein synthesis, amino acid flow and performance of high yielding dairy cows was studied. A significant relationship between the effective degradabilities of OM in feedstuffs and the in vivo ruminal OM degradation of diets of dairy cows was found. The in situ method enabled the prediction of ruminal nutrients degradability response to processing of energy and nitragenous supplements. The AA profile of the rumen undegradable protein was modified by the processing method. In a continuous culture study total N and
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Nadeau, Elisabet, Andrea von Essen, and Anne Kjersti Bakken. Effekt av kvävegödslingsstrategi på gräsvallens avkastning och foderkvalitet vid olika utvecklingsstadier i första skörd. Department of Applied Animal Science and Welfare, Swedish University of Agricultural Sciences, 2024. http://dx.doi.org/10.54612/a.38e4a3v12l.

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Syftet med projektet var att studera effekt av delad kväve(N)-giva och tidpunkt för den sena N-givan innan första skörd på avkastning, kvävebalans och fodervärde med speciellt fokus på råproteinhalt och råproteinets kvalitet i en timotej/ängssvingel vall. En vallfröblandning med 80 % timotej och 20 % ängssvingel såddes 2017 på NIBIO Kvithamar, Trondheim och 2018 på NIBIO Særheim, Stavanger, Norge och på Rådde gård, Länghem, Sverige (Hushållningssällskapet Sjuhärad). En yta av den sådda arealen skördades som förstaårsvall 2018 på NIBIO Kvithamar och som förstaårsvall 2019 på NIBIO Særheim och R
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van Harn, J., A. Rezaei Far, M. M. van Krimpen, J. Phuc, and C. Veiga. Low crude protein diets supplemented with free amino acids in laying hens : effects on performance, egg quality, N-efficiency, N-excretion, economics and diet carbon footprint. Wageningen Livestock Research, 2021. http://dx.doi.org/10.18174/557184.

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Ohad, Nir, and Robert Fischer. Regulation of Fertilization-Independent Endosperm Development by Polycomb Proteins. United States Department of Agriculture, 2004. http://dx.doi.org/10.32747/2004.7695869.bard.

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Arabidopsis mutants that we have isolated, encode for fertilization-independent endosperm (fie), fertilization-independent seed2 (fis2) and medea (mea) genes, act in the female gametophyte and allow endosperm to develop without fertilization when mutated. We cloned the FIE and MEA genes and showed that they encode WD and SET domain polycomb (Pc G) proteins, respectively. Homologous proteins of FIE and MEA in other organisms are known to regulate gene transcription by modulating chromatin structure. Based on our results, we proposed a model whereby both FIE and MEA interact to suppress transcri
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Dickman, Martin B., and Oded Yarden. Regulation of Early Events in Hyphal Elongation, Branching and Differentiation of Filamentous Fungi. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7580674.bard.

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In filamentous fungi, hyphal elongation, branching and morphogenesis are in many cases the key to successful saprophytic and pathogenic fungal proliferation. The understanding of the fungal morphogenetic response to environmental cues is in its infancy. Studies concerning the regulation of fungal growth and development (some of which have been obtained by the participating collaborators in this project) point to the fact that ser/thr protein kinases and phosphatases are (i) involved in the regulation of such processes and (ii) share common structural and functional features between saprophytes
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